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作 者:李杰平[1] 尹晓林[1] 孔佩艳[1] 陈幸华[1] 曾东风[1] 向茜茜[1] 彭贤贵[1]
机构地区:[1]第三军医大学新桥医院血液科,重庆400037
出 处:《中华血液学杂志》2009年第10期672-674,共3页Chinese Journal of Hematology
摘 要:目的总结原发性巨球蛋白血症颅内浸润的诊疗体会。方法对1例原发性巨球蛋白血症颅内浸润(Bing-Neel综合征)患者的临床资料进行分析,并进行相关文献复习,为其诊断和治疗提供思路。结果患者1年前诊断为原发性巨球蛋白血症,治疗中患者出现持续性头痛。颅脑MRI平扫+增强:右侧额颞叶可见一团块状异常占位病变,他呈高信号,增强后病灶强化明显;手术切除肿瘤组织行病理检查示额叶小细胞恶性肿瘤浸润;免疫组化染色检查示淋巴-浆细胞瘤样细胞颅内侵犯。结论原发性巨球蛋白血症颅内浸润罕见,化疗疗效有限,理想的治疗应该是放疗联合化疗。Objective To sum up the clinical experience of the diagnosis and treatment of intracerebral infiltration by monoclonal plasmacytoid cells in Waldenstroem' s macroglobulinemia (Bing-Neel syndrome). Methods The clinical data of the diagnosis and treatment of a case of Bing-Neel syndrome was analyzed. Results A 56-year-old male was diagnosed as Waldenstroem' s macroglobulinemia one year ago, and presented with persistent headache during the treatment period. Magnetic resonance imaging showed a high intensity area on T2-weighed images in the right frontal lobe which was well enhanced by gadoliniumdiethylenetriaminepenta-acetic acid. Infiltration of neoplastic cells was confirmed by biopsy. Immunohistochemieal examination showed that mature plasmacytoid cells in the cerebral parenchyma were immunoglobulin M positive. Conclusion Infiltration in CNS (Bing-Neel syndrome) is uncommon in Waldenstroem' s macroglobnlinemia. As there is no effective therapy for this Bing-Neel syndrome, combination of radiation and chemotherapy shoued be considered for this situation.
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